Frequent occurrence of the CFTR intron 8 (TG)n 5T allele in men with congenital bilateral absence of the vas deferens. [electronic resource]
- European journal of human genetics : EJHG 1995
- 285-93 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
1018-4813
10.1159/000472312 doi
Alleles Cystic Fibrosis Transmembrane Conductance Regulator--genetics DNA Mutational Analysis Electrophoresis, Polyacrylamide Gel--methods Heterozygote Humans Introns Male Mutation Nucleic Acid Denaturation Vas Deferens--abnormalities